The accuracy of RRTMG is verified through comparison to AER's reference radiation code LBLRTM, which is directly validated
with atmospheric measurements provided by high - quality spectral measurements from satellite -, aircraft - and ground - based instruments.
Not exact matches
«We now have an independent
measurement of these emission sources that does not rely on what was known or thought known,» said Chris McLinden, an
atmospheric scientist
with Environment and Climate Change Canada in Toronto and lead author of the study published this week in Nature Geosciences.
All this modelling work, combined
with in situ
measurements (oceanographic campaigns recently carried out as part of the AMOP project) help improve our understanding of the interactions between biogeochemistry,
atmospheric circulation and oceanic circulation.
New
measurements of
atmospheric loss by NASA's MAVEN probe should help scientists determine how a planet
with rushing water and a temperate climate a few billion years ago transformed into a cold, dry desert.
In the new paper, published in the journal Environmental Research Letters, Höglund - Isaksson estimated global methane emissions from oil and gas systems in over 100 countries over a 32 - year period, using a variety of country - specific data ranging from reported volumes of associated gas to satellite imagery that can show flaring, as well as
atmospheric measurements of ethane, a gas which is released along
with methane and easier to link more directly to oil and gas activities.
To remedy this, Sundar Christopher, an
atmospheric scientist at the University of Alabama at Huntsville, compared satellite data
with ground
measurements in well - studied areas.
«This is the only long - term data set
with regular
measurements of ozone - destroying compounds in the stratosphere,» says
atmospheric chemist Darin Toohey of the University of California, Irvine.
Meteorologists have long used a similar technique to integrate
atmospheric and oceanic
measurements with dynamical models, allowing them to forecast the weather.
The NASA Plankton, Aerosol, Cloud, Ocean Ecosystem (PACE) mission,
with a target launch within the next 5 years, aims to make
measurements that will advance ocean and
atmospheric science and facilitate interdisciplinary studies involving the interaction of the atmosphere
with ocean biological systems.
The Aerosol
Measurement Science Group (AMSG) coordinates ARM Facility observations of aerosols and
atmospheric trace gases
with user needs.
Dargaville, R.J., et al., 2002: Evaluation of terrestrial carbon cycle models
with atmospheric CO2
measurements: Results from transient simulations considering increasing CO2, climate, and land - use effects.
Many of the planets discovered by EDEN around nearby stars will be suitable for in - depth
atmospheric characterization, mass, radius, and bulk density
measurements through follow - up observations
with large ground - and space - based telescopes, such as NASA's James Webb Space Telescope.
Ongoing
measurements of anthropogenic CO2, other gases and hydrographic parameters in these key marginal seas will provide information on changes in global oceanic CO2 uptake associated
with the predicted increasing
atmospheric CO2 and future global climate change.
The ARM Aerosol
Measurement Science Group (AMSG) coordinates ARM Climate Research Facility observations of aerosols and
atmospheric trace gases
with user needs to ensure advanced, well - characterized observational
measurements and data products — at the spatial and temporal scales necessary — for improving climate science and model forecasts.
The PEGASOS project will investigate the impacts of European air pollution on climate change and vice versa by combining field
measurements with state of the art
atmospheric and climate models.
We find (i)
measurements at all scales show that official inventories consistently underestimate actual CH4 [methane] emissions,
with the natural gas and oil sectors as important contributors; (ii) many independent experiments suggest that a small number of «super-emitters» could be responsible for a large fraction of leakage; (iii) recent regional
atmospheric studies
with very high emissions rates are unlikely to be representative of typical natural gas system leakage rates; and (iv) assessments using 100 - year impact indicators show system - wide leakage is unlikely to be large enough to negate climate benefits of coal - to - natural gas substitution.
Mike's work, like that of previous award winners, is diverse, and includes pioneering and highly cited work in time series analysis (an elegant use of Thomson's multitaper spectral analysis approach to detect spatiotemporal oscillations in the climate record and methods for smoothing temporal data), decadal climate variability (the term «Atlantic Multidecadal Oscillation» or «AMO» was coined by Mike in an interview
with Science's Richard Kerr about a paper he had published
with Tom Delworth of GFDL showing evidence in both climate model simulations and observational data for a 50 - 70 year oscillation in the climate system; significantly Mike also published work
with Kerry Emanuel in 2006 showing that the AMO concept has been overstated as regards its role in 20th century tropical Atlantic SST changes, a finding recently reaffirmed by a study published in Nature), in showing how changes in radiative forcing from volcanoes can affect ENSO, in examining the role of solar variations in explaining the pattern of the Medieval Climate Anomaly and Little Ice Age, the relationship between the climate changes of past centuries and phenomena such as Atlantic tropical cyclones and global sea level, and even a bit of work in
atmospheric chemistry (an analysis of beryllium - 7
measurements).
Pages 137 - 140 of IPCC AR4 describe high - precision in situ
measurements of
atmospheric CO2 at Mauna Loa, documenting the steady increase in CO2 along
with its characteristic seasonal fluctuation.
... This brings up the nightmarish thought that if the chemical industry had developed organobromine compounds instead of the CFCs — or alternatively, if chlorine chemistry would have run more like that of bromine — then without any preparedness, we would have been faced
with a catastrophic ozone hole everywhere and at all seasons during the 1970s, probably before the
atmospheric chemists had developed the necessary knowledge to identify the problem and the appropriate techniques for the necessary critical
measurements.
The work is an estimate of the global average based on a single - column, time - average model of the atmosphere and surface (
with some approximations — e.g. the surface is not truly a perfect blackbody in the LW (long - wave) portion of the spectrum (the wavelengths dominated by terrestrial /
atmospheric emission, as opposed to SW radiation, dominated by solar radiation), but it can give you a pretty good idea of things (fig 1 shows a spectrum of radiation to space); there is also some comparison to actual
measurements.
Validation of the CO2 inversion product (v16r1): mean bias of the
atmospheric component of this product
with respect to independent aircraft
measurements in the free troposphere.
This product primarily exploits high - quality
measurements of air samples collected at tens of sites around the world by various laboratories (119 sites for CO2, 30 sites for CH4 and 127 sites for N2O), in combination
with a numerical model of
atmospheric tracer transport (Chevallier et al. 2010, Bergamaschi et al. 2013, Thompson et al. 2014).
It is demonstrated that even
with historical SSTs as a boundary condition, most
atmospheric models exhibit excessive tropical upper tropospheric warming relative to the lower - middle troposphere as compared
with satellite - borne microwave sounding unit
measurements.
The work in question takes
measurements from one locale, and doesn't publish conclusions, rather Doney's statements are giving his opinion about what he read, «Long - term ocean acidification trends are clearly evident over the past several decades in open - ocean time - series and hydrographic survey data, and the trends are consistent
with the growth rate of
atmospheric carbon dioxide (Dore et al., 2009).»
Wagner et al.'s conclusion that «during the early Holocene,
atmospheric CO2 concentrations that were > 300 ppmv could have been the rule rather than the exception» conflicts
with other independent
measurements or estimates of CO2concentrations (2 — 5).
In 1990, he joined
with a colleague, Roy Spencer, to use
measurements taken by NASA satellites since 1979 to produce the first global
atmospheric temperature data.
Increases in the rate of anthropogenic emissions of CO2 do not keep pace
with the rate of increases in
atmospheric CO2, because the CO2 from anthropogenic sources are negligible enough to be on the limits of detectable
measurement.
Yet models of
atmospheric absorption that only take into account the water molecule's well - known rotational and vibration - rotational transitions don't match up
with measurements of the atmosphere's absorption spectrum [1]....
Lab
measurements with ejector - type diluters mostly led to bimodal distributions that did not well resemble
atmospheric size distributions.
This (link) is a classic tracer
measurement, where the tracer material (carbon - 14) was in equilibrium
with all the sources / sinks before the
atmospheric a-bomb tests introduced an «impulse» of C - 14 that was abruptly ended
with the
atmospheric test ban treaty of 1963.
Also, there is paleoclimate data that contradicts the ice - core data, such as Stomata and we have 90,000 direct empirical chemical
measurements dating back to 1812 of
atmospheric with a 3 % accuracy that depicts CO2 as high as 440ppm (Beck 2007).
-- robust radiative physics — ground - based instrumental evidence that CO2 absorbs and therefore emits IR exactly in accordance
with the physical theory — satellite data confirming this — satellite data apparently indicating a radiative imbalance at TOA — robust
measurements of the fraction of
atmospheric CO2 — increasing global OHC since the mid-C20th
Even if we could discriminate between human - originated CO2 and natural CO2 isotopically
with reliability I don't see how carbon isotope
measurements could prove we have increased
atmospheric CO2 by 40 % anyway (or 110ppm) because, problematically, CO2 has a very short
atmospheric residence time.
«Since 1990, surface ocean pH has directly been measured or calculated at several locations,
with the average recent decrease estimated as 0.0019 pH units per year at the Hawaii Ocean Time - series (HOT; close to the site of long - term
atmospheric CO2
measurements at Mauna Loa)[12]; 0.0017 per year based on transects in the North Pacific [13]; 0.0012 per year at the Bermuda Atlantic Time - Series (BATS)[14] and 0.0017 per year at the European Station for Time - Series in the Ocean at the Canary Islands (ESTOC)[15].
temperature, other climatic variables, and concentrations of aerosols and trace gases; and (2) making raw and processed
atmospheric measurements accessible in a form that enables a number of different groups to replicate and experiment
with the processing of the more widely disseminated data sets such as the MSU tropospheric temperature record.
On the other hand, theory shows that sulfuric acid / water aerosols are not stable by themselves requiring amines to stabilize and
measurements with an
atmospheric pressure inlet time of flight mass spectrometer showed that the intermediate aerosols did incorporate amines.
The second factor is the insulating effect of the atmosphere of which well over 90 % results from
atmospheric water in the form of clouds and water vapour
with the remaining 10 % due primarily from CO2 and ozone
with just a slightly detectable effect from methane and a trivial effect from all the other gases named in tyhe Kyoto Accord that is so small it can't even be detected on
measurements of the Earth's radiative spectrum.
Also, while we have good
atmospheric measurements of other key greenhouse gases such as carbon dioxide and methane, we have poor
measurements of global water vapor, so it is not certain by how much
atmospheric concentrations have risen in recent decades or centuries, though satellite
measurements, combined
with balloon data and some in - situ ground
measurements indicate generally positive trends in global water vapor.»
However,
measurements of the
atmospheric composition don't show any major change associated
with the troposphere / tropopause transition.
Ernst - Georg Beck, by assembling more than 90,000 pre-1958
measurements of
atmospheric CO2 dating back to the nineteenth century, has shown rather large variations, including a major increase roughly coincident
with a rise in ocean temperatures from 1920 to 1940 [Beck 2007].
In this data activity, students use NASA satellite
measurements of
atmospheric pressure to learn that pressure decreases
with height in the atmosphere.
Consistent
with this, the annual average
atmospheric CO2
measurement stations in the Northern Hemisphere (NH) record slightly higher CO2 concentrations than stations in the Southern Hemisphere (SH).
Combined
with ice core
measurements from Greenland and Antarctica, this tells us that
atmospheric CO2 levels are the highest in over 15 million years (Tripati 2009).
ECMWF has been entrusted to operate two key parts of the Copernicus programme and is assisting
with a third to bring a consistent standard to the
measurement, forecasting and prediction of
atmospheric conditions and climate change:
If» a warmer world will have an atmosphere
with more water vapor,» why has
atmospheric water vapor declined since satellite
measurements began in 1983, and why has tropospheric relative and specific humidity declined since 1948?
One needs to look at the history of the d13C values:
measurements in ice cores, firn and recently direct
atmospheric, show a near steady state of d13C levels in the atmosphere of about -6.3 + / - 0.1 per mil in the period before 1850, decreasing faster and faster after 1850
with a d13C level below -8 per mil nowadays.
This parallels a recent NOAA study of
atmospheric methane
measurements that found that «methane emissions from natural gas as a fraction of production have declined from approximately 8 per cent to approximately 2 per cent over the past three decades» —
with production soaring in recent years.
The ability to hindcast the detailed changes in
atmospheric composition over the past decade, particularly the variability of tropospheric O3 and CO, is limited by the availability of
measurements and their integration
with models and emissions data.
Multilayered
atmospheric temperature
measurement across the earth
with resolutions never before seen.
In a novel application of space - based
atmospheric measurements,
Atmospheric and Environmental Research (AER), in collaboration
with GeoOptics Inc., is investigating the use of radio occultation
measurements to improve severe weather forecasting.